chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
2	230653504	230653505	T	TA	19	GENIC	possibly homozygous	62339361
2	230653956	230653957	G	A	29	GENIC	possibly homozygous	60085434
2	230654770	230654771	C	CTTTTTTT	13	GENIC	heterozygous	60520712
2	230654933	230654934	C	CGGCA	11	GENIC	heterozygous	62058906
2	230656954	230656957	TTT	---	9	GENIC	heterozygous	60520713
2	230656955	230656957	TT	--	9	GENIC	heterozygous	60520714
2	230658581	230658582	T	A	40	GENIC	homozygous	59432458
2	230660599	230660600	C	CTTT	4	GENIC	heterozygous	59775947
2	230661219	230661220	G	GGA	11	GENIC	heterozygous	59432463
2	230662330	230662331	G	GC	21	GENIC	heterozygous	59432467
2	230666172	230666173	A	G	22	GENIC	heterozygous	59432469
2	230666570	230666571	C	T	19	GENIC	homozygous	59432470
2	230667944	230667946	CT	--	5	GENIC	homozygous	59432474
2	230667951	230667952	G	-	5	GENIC	homozygous	59432475
2	230668118	230668119	G	A	15	GENIC	heterozygous	59432476
2	230672185	230672186	C	CAAAGACCCAGGA	23	GENIC	homozygous	59432480
2	230673694	230673695	T	C	7	GENIC	homozygous	59432482
2	230673759	230673760	T	-	6	GENIC	homozygous	60085450
2	230675478	230675479	A	G	13	GENIC	homozygous	59432483
2	230676081	230676082	A	G	25	GENIC	homozygous	59432484
2	230660599	230660600	C	CTTTTT	4	GENIC	heterozygous	60594551